GALACTOSEMIA CLASSICAL (TRANSFERASE), QUANTITATIVE, BLOOD
Classical Galactosemia due to complete deficiency of Galactose -1- phosphate uridyltransferase is characterised by poor growth, mental retardation, speech abnormalities, vison impairment due to cataract and liver enlargement. Partial deficiency of Galactose -1- phosphate uridyltransferase leads to Galactosemia Duarte variant.
Parameter(s) covered : 2
Report Frequency: Sample Daily by 4 pm; Report 5 days
Special Instruction: Avoid sample collection for 60 days post transfusion. Clinical and drug history must accompany sample.
Price : ₹ 2100.00
Parameters
- Control Value
- Patient Value